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Air–Liquid Interface Culture of Human and Mouse Airway Epithelial Cells

  • Di Jiang
  • Niccolette Schaefer
  • Hong Wei Chu
Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 1809)

Abstract

Air–liquid interface culture enables airway epithelial cells to differentiate into a pseudostratified cell layer, consisting of ciliated cells, goblet/secretory cells, and basal cells (Ghio et al., Part Fibre Toxicol 10:25, 2013). This technique is critically important for in vitro studies of lung diseases such as asthma, chronic obstructive pulmonary disease, and cystic fibrosis, since differentiated airway epithelial cells are more representative of the in vivo lung environment than non-differentiated cells (Derichs et al., FASEB J 25:2325–2332, 2011; Hackett et al., Am J Respir Cell Mol Biol 45:1090–1100, 2011;Schneider et al., Am J Respir Crit Care Med 182: 332–340, 2010). Here we describe the process of isolating and expanding human and mouse airway epithelial cells, as well as differentiation of airway epithelial cells by air–liquid interface culture.

Key words

Air–liquid interface Airway epithelial cells Cell differentiation 

Notes

Acknowledgments

The authors thank Max A. Seibold, Reem Al Mubarak, Nicole Roberts, and Reena Berman for their technical assistance in cell culture methodology.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of MedicineNational Jewish HealthDenverUSA

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